FAM13B antibody

Catalog No. ABIN7243301

This anti-FAM13B antibody is a Rabbit Polyclonal antibody detecting FAM13B in ELISA and IHC. Suitable for Human and Mouse.

Quick Overview for FAM13B antibody (ABIN7243301)

Target: FAM13B (Family with Sequence Similarity 13, Member B (FAM13B))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FAM13B antibody is un-conjugated

Application: ELISA, Immunohistochemistry (IHC)

Product Details anti-FAM13B Antibody

Characteristics: Polyclonal Antibody

Purification: Affinity purification

Immunogen: Synthetic peptide of human FAM13B

Isotype: IgG

Application Details

Application Notes: IHC 1:50-1:200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.4 mg/mL

Buffer: PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for FAM13B

Target: FAM13B (Family with Sequence Similarity 13, Member B (FAM13B))

Alternative Name: FAM13B

Background: FAM13B is a 915 amino acid protein that is encoded by a gene that maps to human chromosome 5. With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6 % of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.

NCBI Accession: NP_057687

UniProt: Q9NYF5